摘要
Lysine formylation is a newly discovered post-translational modification (PTM) in histones and other nuclear proteins; it has a well-recognized but poorly defined role in chromatin conformation modulation and gene expression. To date, there is no general method to site-specifically incorporate Nε-formyllysine at a defined site of a protein. Here we report the highly efficient genetic incorporation of the unnatural amino acid Nε-formyllysine into proteins produced in Escherichia coli and mammalian cells, by using an orthogonal Nε-formyllysine tRNAsynthetase/tRNACUA pair. This technique can be applied to study the role of lysine formylation in epigenetic regulation.
| 源语言 | 英语 |
|---|---|
| 页(从-至) | 1440-1442 |
| 页数 | 3 |
| 期刊 | ChemBioChem |
| 卷 | 16 |
| 期 | 10 |
| DOI | |
| 出版状态 | 已出版 - 1 7月 2015 |
| 已对外发布 | 是 |
学术指纹
探究 'Genetic Incorporation of Nε-Formyllysine, a New Histone Post-translational Modification' 的科研主题。它们共同构成独一无二的学术指纹。引用此
- APA
- Author
- BIBTEX
- Harvard
- Standard
- RIS
- Vancouver